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作 者:胡璟[1] 胡可锦[1] 赵素萍[1] 唐瑶云[1]
机构地区:[1]中南大学湘雅医院耳鼻喉科,湖南长沙410008
出 处:《现代生物医学进展》2009年第13期2472-2475,共4页Progress in Modern Biomedicine
基 金:国家自然科学基金资助(30672296);湖南省自然科学基金资助(06JJ4050);高等学校博士学科点专项科研基金资助(20050533014);湖南省卫生厅项目资助(62006152)
摘 要:目的:构建融合启动子E6.hTERTp,以探讨放射干预后放射敏感启动子片段E6对人端粒酶逆转录酶启动子(hTERTp)启动活性以及对鼻咽癌靶向调控的影响。方法:通过Overlap PCR法合成融合启动子E6.hTERTp,连接至PGL3 basic质粒。构建含EGR-1启动子(EGR-1p)以及hTERTp的PGL3 basic载体做对照。使用Lipo2000将报告载体以及pRL-SV40质粒共转染正常人成纤维细胞HDF以及人鼻咽癌CNE-2细胞,并给予不同剂量放射干预,双荧光素酶法检测其启动活性。t检验分析不同细胞系中不同放射条件下各启动子启动活性差别。结果:在正常HDF细胞系内,无论放射与否,hTERTp组以及E6.hTERTp组的启动活性均很低;而在CNE2细胞系中,三种启动子启动活性均随放射剂量增加而增加,其增长幅度从大到小分别是EGR-1p组、E6.hTERTp组、hTERTp组。在相同放射剂量干预下,EGR-1P组、E6.hTERTp组与hTERTp组三组间的启动活性两两之间均有统计学差别(p<0.01)。结论:放射诱导型增强子E6能够明显提高hTERTp放射敏感性,且不影响其在鼻咽癌中靶向性调控作用,为该类肿瘤的放射-基因治疗提供了新的思路。Objective: Construct novel promotor E6.hTERTp to detect the influence of radiosensitive enhancer E6 to hTERTp's targeting promotive effect. Methods: The fusion gene E6.hTERTp was constructed by overlap PCR and was inserted into PGL3 basic plasmid. PGL3-hTERTp and pGL3-EGRlp were also constructed for comparison. All the plasmids together with pRL-SV40 plasmids were transfected into CNE-2 cells and HDF cells with liposome .The promotive effect of recombinant promoter E6.hTERTp in CNE-2 cells and HDF cells were measured by dual luciferase reporter gene assay system and was compared with EGR-Ip and hTERTp for difference between every two groups under different dose of radiation .The results were analyzed with t test; Results: The promotive effects of hTERT promoter and E6.hTERTp were absent in HDF cells with any dose of radiation; While in CNE-2 cells, increase of promotive effects in accordance with the radiation dose could be observed in all groups. The change to baseline (0Gy) in descending sequence were the EGR-1p group; the E6.hTERTp group and the hTERTp group; under the same dose of radiation, the difference between the promo- tive effect of EGR-1p, E6.hTERTp group and hTERTp group were statistically significant(p〈0.01 ). Conclusion: Radiosensitive enhancer E6 increases the radiosensitive promotive effect of hTERTp in CNE-2 cells and does not decrease its NPC targeting character. This can be a potential strategy of radio-gene therapy for tumors mainly treated by radiation.
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